Ann Smart Martin

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Analyzing the type and frequency of patient-specific mutations that give rise to Duchenne muscular dystrophy (DMD) is an invaluable tool for diagnostics, basic scientific research, trial planning, and improved clinical care. Locus-specific databases allow for the collection, organization, storage, and analysis of genetic variants of disease. Here, we(More)
My primary goal in compiling this bibliography is to explore ways that scholars use objects to learn about people, their ideas, and their experiences. Objects are defined broadly to include things, buildings, and landscapes. Works have been chosen to represent a wide range of approaches and their disciplinary development over the last fifty years. I have(More)
Our study objective was to survey female carriers for Duchenne and Becker muscular dystrophy to identify barriers to carrier testing and the impact of carrier risk knowledge on cardiac and reproductive health management. We surveyed women who have or had biological sons with Duchenne or Becker muscular dystrophy and were enrolled in the US DuchenneConnect(More)
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